Vol. 12 No. 2 (2011) | Egyptian Journal of Medical Human Genetics

Models to explore the molecular function and regulation of AIRE

T Lovewell, R Tazi-Ahnini

107-115

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Hereditary periodic fever syndromes

RM Shawky, NEA Gaboon

117-125

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Correlation between the RhD genotyping and RhD serotyping in isoimmunized pregnancies

SM Nour El Din, ARM ARamy, MS Ali

127-133

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Role of ZIP14 (SLC39A14) gene histidine rich regions in neural tube defects

D Torun, E Yılmaz, E Akar, N Akar

135-137

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Serum interferon-alpha level in first degree relatives of systemic lupus erythematosus patients: Correlation with autoantibodies titers

D Shahin, AM El-Refaey, AK El-Hawary, AA Salam, S Machaly, N Abousamra, RM El-farahaty

139-146

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Low bone density management via capacitively coupled electrical fields and low intensity pulsed ultrasound in hemiparetic cerebral palsy

KA Olama

147-150

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Genetic association between common beta-2 adrenoreceptor polymorphism and asthma severity in school-age children

MS Salama, NA Ashaat, AA Hamad

151-156

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Consanguineous matings among Egyptian population

RM Shawky, MY El-Awady, SM Elsayed, GE Hamadan

157-163

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Serine protease (TPS): A diagnostic and prognostic marker in pediatric patients with acute non-lymphoblastic leukemia

SHA Agwa, NS El-Kinawy, AA Shuoyb

165-170

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Ocular features in Egyptian genetically disabled children

GR El-Hawary, RM Shawky, AS El-Din, SMN El-Din

171-181

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Thiopurine S-methyltransferase genetic polymorphism in the Tunisian population

LB Salah, CB Salem, F B’Chir, K Bouraoui, F Broly, S Saguem

183-186

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Null genetic risk of ACE gene polymorphisms with nephropathy in type 1 diabetes among Egyptian population

NA Elhawary, N Bogari, M Rashad, MT Tayeb

187-192

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Endurance exercises versus treadmill training in improving muscle strength and functional activities in hemiparetic cerebral palsy

KA Olama

193-199

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Molecular detection of circulating thyroid specific transcripts (TSHR/Tg-mRNAs) in thyroid cancer patients: Their diagnostic significance

SH Teama, SHA Agwa, A Fawzy, MM Sayed, WA Ibrahim, YM Eid

201-209

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Salivary PCR detection of Helicobacter pylori DNA in Egyptian patients with dyspepsia

MM Sayed, WA Ibrahim, SA Abdel-bary, SM Abdelhakam, SA El-Masry, D Ghoraba

211-216

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Goldenhar syndrome with skin tags on the chest wall

RM Shawky, SS Zahra

217-220

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Egyptian Journal of Medical Human Genetics
Journal / Egyptian Journal of Medical Human Genetics / Vol. 12 No. 2 (2011) / Articles

Articles

Models to explore the molecular function and regulation of AIRE

Hereditary periodic fever syndromes

Correlation between the RhD genotyping and RhD serotyping in isoimmunized pregnancies

Role of ZIP14 (SLC39A14) gene histidine rich regions in neural tube defects

Serum interferon-alpha level in first degree relatives of systemic lupus erythematosus patients: Correlation with autoantibodies titers

Low bone density management via capacitively coupled electrical fields and low intensity pulsed ultrasound in hemiparetic cerebral palsy

Genetic association between common beta-2 adrenoreceptor polymorphism and asthma severity in school-age children

Consanguineous matings among Egyptian population

Serine protease (TPS): A diagnostic and prognostic marker in pediatric patients with acute non-lymphoblastic leukemia

Ocular features in Egyptian genetically disabled children

Thiopurine S-methyltransferase genetic polymorphism in the Tunisian population

Null genetic risk of ACE gene polymorphisms with nephropathy in type 1 diabetes among Egyptian population

Endurance exercises versus treadmill training in improving muscle strength and functional activities in hemiparetic cerebral palsy

Molecular detection of circulating thyroid specific transcripts (TSHR/Tg-mRNAs) in thyroid cancer patients: Their diagnostic significance

Salivary PCR detection of Helicobacter pylori DNA in Egyptian patients with dyspepsia

Goldenhar syndrome with skin tags on the chest wall

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